| Literature DB >> 27176914 |
Jian Zhang1, Xiaolong Bao1, Junliang Zhou1, Fangfang Peng2, Hang Ren1, Xiaochun Dong1, Weili Zhao3.
Abstract
A novel turn-on red fluorescent BODIPY-based probe (Probe 1) for the detection of glutathione was developed. Such a probe carries a para-dinitrophenoxy benzyl pyridinium moiety at the meso position of a BODIPY dye as self-immolative linker. Probe 1 responds selectively to glutathione with the detection limit of 109nM over other amino acids, common metal ions, reactive oxygen species, reactive nitrogen species, and reactive sulfur species. A novel electrostatic interaction to modulate the SNAr attack of glutathione was believed to play significant role for the observed selective response to glutathione. The cleavage of dinitrophenyl ether by glutathione leads to the production of para-hydroxybenzyl moiety which is able to self-immolate through an intramolecular 1,4-elimination reaction to release the fluorescent BODIPY dye. The low toxic probe has been successfully used to detect mitochondrial glutathione in living cells.Entities:
Keywords: BODIPY; Fluorescence imaging; Fluorescent probe; Glutathione; Mitochondria-targeted
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Year: 2016 PMID: 27176914 DOI: 10.1016/j.bios.2016.05.005
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618